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  2. N-cyclohexyl-1-(2,4-dichlorophenyl)-6-methyl-4H-indeno[1,2-c]pyrazole-3-carboxamide

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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

N-cyclohexyl-1-(2,4-dichlorophenyl)-6-methyl-4H-indeno[1,2-c]pyrazole-3-carboxamide

Cc1ccc2c(c1)Cc1c2n(nc1C(=O)NC1CCCCC1)c1ccc(cc1Cl)Cl Request for Quotation
Chemical Name: N-cyclohexyl-1-(2,4-dichlorophenyl)-6-methyl-4H-indeno[1,2-c]pyrazole-3-carboxamide
CAS Number: 919077-81-9
Product Number: AG00H0B2(AGN-PC-00SXCG)
Synonyms:
MDL No: MFCD09971118
Molecular Formula: C24H23Cl2N3O
Molecular Weight: 440.3649

Identification/Properties

Computed Properties
Molecular Weight:
440.368g/mol
XLogP3:
6.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
439.122g/mol
Monoisotopic Mass:
439.122g/mol
Topological Polar Surface Area:
46.9A^2
Heavy Atom Count:
30
Formal Charge:
0
Complexity:
628
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


GP 2A is a versatile reagent commonly utilized in chemical synthesis for obtaining high-purity products. Its unique properties make it an essential tool in organic chemistry, particularly in the formation of complex organic compounds. GP 2A is known for its ability to facilitate a variety of transformations, including cross-coupling reactions, C-H activation, and functional group interconversions. Additionally, its compatibility with a wide range of functional groups and substrates makes it a valuable resource for synthetic chemists aiming to streamline their processes and improve overall efficiency. By enabling selective and controlled bond formations, GP 2A plays a crucial role in the synthesis of valuable pharmaceuticals, agrochemicals, and materials with enhanced properties. Its remarkable performance and reliability make it a go-to reagent for researchers seeking to achieve precise and reproducible results in their synthetic endeavors.